Gavin Hudson

11.4k citations

81 papers · 4.5k indexed · 1 hit paper · h-index 37

Impact in

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
Neurology top 1%
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments

Papers in

Clinical Biochemistry 30
- Metabolism and Genetic Disorders 30
Neurology 19
- Parkinson's Disease Mechanisms and Treatments 13
- Neurological diseases and metabolism 4

Co-authors: Patrick F. Chinnery Philip G. Griffiths Angela Pyle Patrick Yu‐Wai‐Man David J. Burn Robert W. Taylor Alison J. Yarnall Douglass M. Turnbull
Journals: Neurology (7 papers)Mitochondrion (6 papers)PLoS Genetics (5 papers)Movement Disorders (4 papers)Neuromuscular Disorders (4 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Gavin Hudson

80 papers receiving 4.4k citations

Hit Papers

align trajectories log scale

Characterizing mild cognitive impairment in incident Parkinson disease 2013 · 330 citations

Peers

Countries citing papers authored by Gavin Hudson

Since Specialization

Citations

This map shows the geographic impact of Gavin Hudson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gavin Hudson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gavin Hudson more than expected).

Fields of papers citing papers by Gavin Hudson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gavin Hudson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gavin Hudson. The network helps show where Gavin Hudson may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Gavin Hudson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Gavin Hudson Line = papers co-authored together Gavin Hudson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Early-stage idiopathic Parkinson’s disease is associated with reduced circular RNA expression npj Parkinson s Disease ·이세진, Osagie Izuogu, H. ERTON, E. Pajot, Angela Pyle, Ivan Pineda Velasco, Rachael A. Lawson, Alison J. Yarnall, Michael S. Jackson, Mauro Santibanez‐Koref, Gavin Hudson	2024	11
2	Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues Scientific Reports ·Сергій МАЦЮК, Angela Pyle, Amy E. Vincent, Paolo Actis, Gavin Hudson	2024	1
3	Genomic Strategies in Mitochondrial Diagnostics Methods in molecular biology ·E. Pajot, Charlotte L. Alston, Gavin Hudson, Robert W. Taylor, Angela Pyle	2023	0
4	Feasibility and impact of haplogroup matching for mitochondrial replacement treatment EMBO Reports ·Yuko Takeda, Louise Hyslop, Meenakshi Choudhary, Fiona Robertson, Angela Pyle, Ian Wilson, Mauro Santibanez‐Koref, Douglass M. Turnbull, Mary Herbert, Gavin Hudson	2023	3
5	A subcellular cookie cutter for spatial genomics in human tissue Analytical and Bioanalytical Chemistry ·Сергій МАЦЮК, Angela Pyle, L. H. Luttrull, Douglass M. Turnbull, Amy E. Vincent, Gavin Hudson, Paolo Actis	2022	9
6	GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10‐Year Population‐Based Study Movement Disorders ·P. K. Vrinda, Ingvild Dalen, Kenn Freddy Pedersen, Marta Camacho, David Bäckström, Lars Forsgren, Charalampos Tzoulis, Sophie Winder‐Rhodes, Gavin Hudson, Ganqiang Liu, Clemens R. Scherzer, Rachael Lawson, Alison J. Yarnall, Caroline H. Williams‐Gray, Angus D. Macleod, Carl Counsell, Ole‐Bjørn Tysnes, Guido Alves, Jodi Maple‐Grødem	2022	71
7	The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi‐omic pipelines The Journal of Pathology ·Charlotte L. Alston, Sarah L. Stenton, Gavin Hudson, Holger Prokisch, Robert W. Taylor	2021	36
8	Mutations in mitochondrial DNA causing tubulointerstitial kidney disease PLoS Genetics ·Thomas M. Connor, Simon Hoer, Andrew J. Mallett, Daniel P. Gale, Aurora Gómez-Durán, Viktor Posse, Robin Antrobus, Pablo Moreno, Marco Sciacovelli, Christian Frezza, Jennifer Duff, Neil Sheerin, John A. Sayer, Margaret Ashcroft, Michael S. Wiesener, Gavin Hudson, Claes M. Gustafsson, Patrick F. Chinnery, Patrick H. Maxwell	2017	40
9	Exome sequencing in dementia with Lewy bodies Translational Psychiatry ·Michael J. Keogh, Marzena Kurzawa‐Akanbi, Helen Griffin, Konstantinos Douroudis, Kristin L. Ayers, 誠二早川, Gavin Hudson, Angela Pyle, Heather J. Cordell, Johannes Attems, Ian G. McKeith, John T. O’Brien, David J. Burn, Christopher M. Morris, Yu MengYang, Patrick F. Chinnery	2016	34
10	Variation in complement protein C1q is not a major contributor to cognitive impairment in Parkinson’s disease Neuroscience Letters ·Bryan Walsh, Jennifer Duff, Alison J. Yarnall, David J. Burn, Gavin Hudson	2015	10
11	Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans PLoS Genetics ·Angela Pyle, Gavin Hudson, Ian Wilson, Jonathan Coxhead, Michelle M. Hood, Mary Herbert, Mauro Santibanez‐Koref, Patrick F. Chinnery	2015	55
12	Recent Mitochondrial DNA Mutations Increase the Risk of Developing Common Late-Onset Human Diseases PLoS Genetics ·Gavin Hudson, Aurora Gómez-Durán, Ian Wilson, Patrick F. Chinnery	2014	113
13	Raised Intraocular Pressure as a Potential Risk Factor for Visual Loss in Leber Hereditary Optic Neuropathy PLoS ONE ·Anaïs Thouin, Philip G. Griffiths, Gavin Hudson, Patrick F. Chinnery, Patrick Yu‐Wai‐Man	2013	21
14	Mitochondrial genetics British Medical Bulletin ·Patrick F. Chinnery, Gavin Hudson	2013	278
15	Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON Mitochondrion ·Gavin Hudson, Patrick Yu‐Wai‐Man, Philip G. Griffiths, Rita Horváth, Valério Carelli, Massimo Zeviani, Patrick F. Chinnery	2011	4
16	Leber hereditary optic neuropathy Expert Opinion on Medical Diagnostics ·Gavin Hudson, Patrick Yu‐Wai‐Man, Patrick F. Chinnery	2008	48
17	Mutation of the Linker Region of the Polymerase γ-1 (POLG1Gene Associated With Progressive External Ophthalmoplegia and Parkinsonism Archives of Neurology ·Gavin Hudson, Andrew M. Schaefer, Robert W. Taylor, Watcharee Tiangyou, Andrew Gibson, 胡永林, Philip G. Griffiths, David J. Burn, Douglass M. Turnbull, Patrick F. Chinnery	2007	66
18	Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance Brain ·Gavin Hudson, Patrizia Amati‐Bonneau, Emma L. Blakely, Joanna D. Stewart, Langping He, Andrew M. Schaefer, Philip G. Griffiths, Kati J. Ahlqvist, Anu Suomalainen, Pascal Reynier, Robert McFarland, Douglass M. Turnbull, Patrick F. Chinnery, Robert W. Taylor	2007	304
19	Mutant POLG2 Disrupts DNA Polymerase γ Subunits and Causes Progressive External Ophthalmoplegia The American Journal of Human Genetics ·Matthew J. Longley, Rahaf Alsubey, Cynthia Yu‐Wai‐Man, Gavin Hudson, Steve E. Durham, Robert W. Taylor, Simon Nightingale, Douglass M. Turnbull, William C. Copeland, Patrick F. Chinnery	2006	175
20	Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder The American Journal of Human Genetics ·Gavin Hudson, Sharon Keers, Patrick Yu Wai Man, Philip G. Griffiths, Kirsi Huoponen, Marja-Liisa Savontaus, Eeva Nikoskelainen, Massimo Zeviani, Franco Carrara, Rita Horváth, Veronika Karcagi, Liesbeth Spruijt, I.F.M. de Coo, Hubert J.M. Smeets, Patrick F. Chinnery	2005	144

About Gavin Hudson

Gavin Hudson is a scholar working on Clinical Biochemistry, Neurology, Molecular Biology, Neurology and Ophthalmology, having authored 81 papers that have together received 4.5k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (57 papers), Metabolism and Genetic Disorders (30 papers), Parkinson's Disease Mechanisms and Treatments (13 papers), Genetic Neurodegenerative Diseases (11 papers), Metabolomics and Mass Spectrometry Studies (9 papers), ATP Synthase and ATPases Research (9 papers), Drug-Induced Ocular Toxicity (6 papers) and Neurological diseases and metabolism (4 papers). The work is most often cited by research in Clinical Biochemistry (1.4k citations), Neurology (869 citations), Molecular Biology (3.3k citations), Neurology (335 citations) and Aging (60 citations). Gavin Hudson has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Patrick F. Chinnery, Philip G. Griffiths, Angela Pyle, Patrick Yu‐Wai‐Man, David J. Burn, Robert W. Taylor, Alison J. Yarnall, Douglass M. Turnbull, Marzena Kurzawa‐Akanbi and Mauro Santibanez‐Koref. Their work appears in journals such as Neurology, Mitochondrion, PLoS Genetics, Movement Disorders and Neuromuscular Disorders.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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